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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2019 | 2 |
2021 | 1 |
2022 | 2 |
2023 | 1 |
2024 | 0 |
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6 results
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Page 1
Retinal α-synuclein deposits in Parkinson's disease patients and animal models.
Acta Neuropathol. 2019 Mar;137(3):379-395. doi: 10.1007/s00401-018-01956-z. Epub 2019 Feb 5.
Acta Neuropathol. 2019.
PMID: 30721408
Review.
Photosensitive Melanopsin-Containing Retinal Ganglion Cells in Health and Disease: Implications for Circadian Rhythms.
Lax P, Ortuño-Lizarán I, Maneu V, Vidal-Sanz M, Cuenca N.
Lax P, et al.
Int J Mol Sci. 2019 Jun 28;20(13):3164. doi: 10.3390/ijms20133164.
Int J Mol Sci. 2019.
PMID: 31261700
Free PMC article.
Review.
Item in Clipboard
Inherited Retinal Dystrophies: Role of Oxidative Stress and Inflammation in Their Physiopathology and Therapeutic Implications.
Pinilla I, Maneu V, Campello L, Fernández-Sánchez L, Martínez-Gil N, Kutsyr O, Sánchez-Sáez X, Sánchez-Castillo C, Lax P, Cuenca N.
Pinilla I, et al.
Antioxidants (Basel). 2022 May 30;11(6):1086. doi: 10.3390/antiox11061086.
Antioxidants (Basel). 2022.
PMID: 35739983
Free PMC article.
Review.
Item in Clipboard
Microglia activation and neuronal alterations in retinas from COVID-19 patients: correlation with clinical parameters.
Albertos-Arranz H, Martínez-Gil N, Sánchez-Sáez X, Noailles A, Monferrer Adsuara C, Remolí Sargues L, Pérez-Santonja JJ, Lax P, Calvo Andrés R, Cuenca N.
Albertos-Arranz H, et al.
Eye Vis (Lond). 2023 Mar 1;10(1):12. doi: 10.1186/s40662-023-00329-2.
Eye Vis (Lond). 2023.
PMID: 36855168
Free PMC article.
Item in Clipboard
Purinergic Receptors P2X7 and P2X4 as Markers of Disease Progression in the rd10 Mouse Model of Inherited Retinal Dystrophy.
Martínez-Gil N, Kutsyr O, Noailles A, Fernández-Sánchez L, Vidal L, Sánchez-Sáez X, Sánchez-Castillo C, Lax P, Cuenca N, García AG, Maneu V.
Martínez-Gil N, et al.
Int J Mol Sci. 2022 Nov 25;23(23):14758. doi: 10.3390/ijms232314758.
Int J Mol Sci. 2022.
PMID: 36499084
Free PMC article.
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Phenotypic Differences in a PRPH2 Mutation in Members of the Same Family Assessed with OCT and OCTA.
Albertos-Arranz H, Sánchez-Sáez X, Martínez-Gil N, Pinilla I, Coco-Martin RM, Delgado J, Cuenca N.
Albertos-Arranz H, et al.
Diagnostics (Basel). 2021 Apr 26;11(5):777. doi: 10.3390/diagnostics11050777.
Diagnostics (Basel). 2021.
PMID: 33925984
Free PMC article.
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